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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587369Generated: November 4, 2026

1-Benzyl-4-(ethoxycarbonyl)-1-azoniabicyclo[2.2.1]heptane bromide → Ethyl 1-azabicyclo[2.2.1]heptane-4-carboxylate hydrobromide

https://huagongshe.com/reaction/1587369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(ethoxycarbonyl)-1-azoniabicyclo[2.2.1]heptane bromideHCID 22922780—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 1-azabicyclo[2.2.1]heptane-4-carboxylate hydrobromideHCID 2292278684.3%

Reaction Steps

A suspension of ethyl 1-benzyl-1-azoniabicyclo[2.2.1]hept-4-ylcarboxylate bromide (D12, 130 g, 0.38 mole) in ethanol (500 ml) was hydrogenated over 10% palladium on charcoal catalyst (8 g) at atmospheric temperature and pressure for 18 h. The catalyst was removed by filtering through celite, washing several times with hot ethanol, and the filtrate concentrated in vacuo to give the title compound (D13) as a crystalline white solid (80.1 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217975
Source datasetuspto-grants-1993_06
ORD IDord-680b660fb8294e60b9b8ce26a488b508
Source noteuspto-grants-1993_06